
How can you see changing the lives of patient starting taking Nexviazyme and if you can share from your experience couple of patient stories that realy impacted positively from staring the treatment for Pompe disease?
From your experience
This website is intended exclusively for healthcare professionals residing and/or working in the UAE.


From your experience

The End

Advances in Therapy: Avalglucosidase Alfa & Future Innovations


Current Treatment Landscape & hands on Experience




Today we speak with Dr. Nadia Alhashmi, Senior Consultant in Chemical & Bio-Chemical Genetics at the National Genetics Royal Hospital in Oman, and Dr. Khalid Althihli, Senior Consultant in Chemical & Bio-Chemical Genetics at Sultan Qaboos University Hospital in Oman. With deep expertise in rare metabolic and genetic disorders, both specialists bring frontline clinical perspectives on Pompe disease — covering the typical patient journey, diagnostic challenges, and new diagnostic technologies, while sharing their compassionate approach to supporting patients and families and addressing the social stigma surrounding rare diseases.

Welcome to the Pompe Care podcast series. Today we speak with Dr. Rawda Sunbul, Consultant Medical Genetics at Qatif Central Hospital in Saudi Arabia, about Pompe disease. We discuss the typical patient journey and diagnostic challenges. Dr. Sunbul shares insights on new diagnostic technologies, effective ways to support patients and families, and how to address the social stigma surrounding rare diseases.
Differentail Diagnosis for Unspecific Limb - Girdle Muscular Dystrophy (LGMD)/ Dr. Alanood Alsolaihim
It's Not Just A Wakness/ Dr. Ahmed Bamaga




Welcome to Pompe Care podcast series, today’s episodes we speak to Dr. Amal Al Teneiji, Metabolic Genetics Consultant at Sheikh Khalifa Medical City Abu Dhabi, about Pompe disease. We talk about typical diagnosis of patient journey, challenges facing, new diagnostic technologies, effective ways to support patients and families and social stigma.



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